Clinical utility of indigenously formulated single-vial lyophilized HYNIC-TOC kit in evaluating Gastro-entero Pancreatic neuro endocrine tumours.

OBJECTIVES
The objective of this study was to evaluate the performance and utility of (99m)Tc HYNIC-TOC planar scintigraphy and SPECT/CT in the diagnosis, staging and management of gastroenteropancreatic neuroendocrine tumors (GPNETs).


METHODS
22 patients (median age, 46 years) with histologically proven gastro- entero- pancreatic NETs underwent (99m)Tc HYNIC-TOC whole body scintigraphy and regional SPECT/CT as indicated. Scanning was performed after injection of 370-550 MBq (10-15 mCi) of (99m)Tc HYNIC-TOC intravenously. Images were evaluated by two experienced nuclear medicine physicians both qualitatively as well as semi quantitatively (tumor to background and tumor to normal liver ratios on SPECT -CT images). Results of SPECT/CT were compared with the results of conventional imaging. Histopathology results and follow-up somatostatin receptor scintigraphy with (99m)Tc HYNIC TOC or conventional imaging with biochemical markers were considered to be the reference standards.


RESULTS
(99m)Tc HYNIC TOC showed sensitivity and specificity of 87.5% and 85.7%, respectively, for primary tumor and 100% and 86% for metastases. It was better than conventional imaging modalities for the detection of both primary tumor (P<0.001) and metastases (P<0.0001). It changed the management strategy in 6 patients (31.8%) and supported management decisions in 8 patients (36.3%).


CONCLUSION
(99m)Tc HYNIC TOC SPECT/CT appears to be a highly sensitive and specific modality for the detection and staging of GPNETs. It is better than conventional imaging for the evaluation of GPNETs and can have a significant impact on patient management and planning further therapeutic options.


Introduction
Neuroendocrine tumors (NETs), generally considered to be an uncommon entity of neoplasms originating from the neural crest, located mainly in the gastroenteropancreatic tract and lung; with occasional reports of ovarian and thymic origin (1). GPNETs though generally slow-growing, with an asymptomatic and indolent course over many years, many GPNETs are malignant and the patients can present with symptoms related to the primary tumor mass or metastases (2)(3)(4) 30-41. 31 survival (5)(6)(7). Complete surgical excision is the treatment of choice for patients with NET, but in many patients such treatment is not possible at diagnosis; with liver being the most common site of metastases (8)(9)(10). On a case by case basis, various palliative treatments are offered, such as surgical debulking where the symptoms are related to tumors, chemotherapy or interferons for systemic control, intra arterial chemo or radio embolisation for hepatic metastases. However these treatments have only a limited role in symptomatic improvement and in partial tumor regression (11,12). This is an area where somatostatin analogs have played a significant role in not only diagnosis and staging, but also in identifying a potential molecular level target which can be utilized for therapeutic purposes. Thus, highlevel of somatostatin receptor expression makes NETs amenable to treatment using peptide receptor radionuclide therapy in surgically inoperable cases and in advanced cases (13). Conventional imaging modalities such as CT, ultrasound and MRI have largely been replaced by Somatostatin receptor scintigraphy (SSTRI) for both staging, therapy planning and even for follow up imaging (14). Somatostatin, a cyclic peptide hormone consisting of 14 amino acids, acts on tissues through specific receptors that are present in the central nervous system, gastrointestinal tract, and on many cells of neuroendocrine and non-neuroendocrine origin (15).
Overexpression of these receptors has been identified in a wide range of malignant neoplasms. The expression of somatostatin receptors by NETs has led to the use of peptide receptor scintigraphy with radiolabeled somatostatin analogs for imaging. Somatostatin analogues are original hormone molecules which have been modified in various ways, usually in a form shortened to eight amino acids (octapeptides), while preserving most of the biological activity of the original hormone and are less susceptible to enzymatic degradation. They are applicable for diagnostic purposes, as they are stable much longer in vivo and are metabolically stable in the human body (their half-life may reach several hours) (16). At present, five types of somatostatin receptors (SSTR) have been identified. The native somatostatin shows affinity for all of them; the analogues, however, show substantial variation in this respect (17).
In recent years, attempts have been made to develop an analogue with an affinity for all receptor types because, at least one subtype is over expressed in the majority of tumors (18). There is an extensive amount of data in the literature demonstrating that the scintigraphic imaging of somatostatin positive tumors is possible using Octreoscan (Mallinckrodt, Petten, The Netherlands), that is, a conjugate of octreotide labelled with 111 In -DTPA. This tracer enables the scintigraphic imaging of neuroendocrine tumors, which are difficult to detect with other imaging modalities (19,20). However, the use of this radiopharmaceutical has substantial drawbacks: (1) the high cost of the cyclotron produced radionuclide, as well as its suboptimal physical characteristics and (2) the energy of emitted gamma rays makes it suboptimal for scintigraphy. In addition, the physical half-life of 68 hours of 111 In causes a relatively high radiation exposure of patients and has the drawback of limited resolution of SPECT technology and uneven biodistribution of the radiotracer in the liver and spleen, obscuring small lesions.
Attempts to eliminate these drawbacks led, a few years ago, to the synthesis of depreotide, another small peptide, which, in contrast to octapeptides, can be directly labeled with 99m Tc. This radiopharmaceutical, known under the commercial name of Neotect (Schering), is now being used mostly for differential diagnostics of malignant from benign solitary pulmonary nodules (21)(22)(23). Availability of 68 Ga isotope, a generator-derived positron-emitting radionuclide that can be easily labeled to macrocyclic chelators such as DOTA (1, 4, 7, 10tetraaz-acyclododecane-1, 4, 7, 10-tetraacetic acid) has made possible the development of new PET radiotracers for the detection of somatostatin receptors with greater specificity.
Recently, numerous communications on preclinical studies and clinical trials of other 99m Tc labeled somatostatin analogues appeared; mostly octapeptides bound to 99m Tc via special chelators (24)(25)(26)(27)(28)(29)(30)(31)(32)(33). All of these studies were aimed at a radiopharmaceutical showing a high affinity for the maximum number of receptor subtypes, as well as optimal pharmacokinetic characteristics. A new somatostatin analogue applied in this study, a Tyr3-octreotide (TOC) labeled with 99m Tc has been developed by Maecke and Béhé for its favorable preclinical characteristics. These preclinical data were confirmed by Decristoforo and Mather, and their early clinical studies recently appeared (33,34).We have utilized the newly developed lyophilised kits from Bhabha Atomic Research 32 Asia Oceania J Nucl Med Biol. 2014; 2(1): 30-41. Centre (BARC) for the preparation of 99m Tc Hynic TOC and report on their utility in GPNETS. The aim of this study was to assess the performance and obtain indications on the potential clinical usefulness of scintigraphy with the new 99m Tc Hynic TOC radiopharmaceutical in GPNET's. The more specific purpose was to see whether it is possible to detect primary tumors and metastases of somatostatin receptor positive tumors and utilize it for therapy planning with 177 Lu labeled peptides.

Subjects
This was a prospective study. A total of 22 patients with histologically proven GPNETs were evaluated with 99m Tc Hynic TOCSPECT/CT between October 2012 and April 2013. Only the staging planar and SPECT/CT studies were used for the analysis; follow-up studies were excluded. This study was conducted in accordance with our institute's ethics protocol after obtaining ethics committee approval and written informed consent was obtained from all patients. The results of 99m Tc Hynic TOC planar and SPECT/CT were analyzed from the following perspectives: staging disease in patients with already diagnosed NET, detecting sites of recurrence in patients with treated NET (restaging), diagnosing NET in patients suspected of having NET on the basis of clinical features or biochemical results, comparing SPECT/CT results with the results of conventional imaging modalities, selecting potential candidates for peptide-based radioreceptor therapy (PRRT), and establishing whether the results of 99m Tc Hynic TOC SPECT/CT have an impact from a management point of view.

Radiopharmaceutical Preparation
Lyophilized Hynic TOC kit vials were obtained as gift from Radiopharmaceuticals Division, Bhabha Atomic Research Centre (Mumbai). Detailed procedure for the preparation of Hynic TOC kit will be reported elsewhere. Each lyophilized kit vial contains Hynic TOC (30 µg), EDDA (10 mg), tricine (20 mg), sodium phosphate dibasic heptahydrate (4.5 mg), sodium phosphate monobasic (1 mg) and stannous chloride dehydrate (40 µg). The lyophilized kits were subjected to thorough quality control checks, including bacterial endotoxin test and sterility test, at the manufacturer's end before releasing for clinical use.
The radiolabeling procedure was performed under aseptic conditions. 99m Tc-Hynic TOC was prepared by adding 10 -60 mCi (370 -2220 MBq) of freshly eluted sterile 99m Tc-sodium pertechnetate in 1-3 mL of saline, obtained from 99 Mo/ 99m Tc alumina column generator (Radioisotope Centre POLATOM), into the kit vial and heating the vial in boiling water bath for 20 min.
Quality control of the preparation was performed using ITLC-SG (Varian USA) About 2 µL of the test solution was spotted on two separate ITLC-SG strips (10 cm long) at 1.5 cm from the bottom of the strip. One of the strips was developed in methyl ethyl ketone (Strip A) in which pertechnetate moves with the solvent front while 99m Tc-Hynic TOC and reduced Technetium ( 99m TcO 2 ) remains at the point of spotting. The other strip was developed in acetonitrile: water (1:1, v/v) (Strip B) where the 99m Tc-Hynic TOC as well as pertechnetate moves with the solvent front while reduced Technetium remains at the point of spotting. When the developing solvent front reaches about 1 cm from the top of the strip, the strips were removed from the TLC jar, dried, cut into two equal segments and activity associated with each segment was determined in a NaI(Tl) counter with the energy window set for 99m Tc. The labeling yield in all cases exceeded 90%. The radiochemical purity determined in any of the procedures varied between 92% and 98%, with the free pertechnetate content in the range of 1.54% to 2.93%. Sterility and pyrogenicity testing was done by the supplier (BARC) prior to despatch of the kits to our centre.

Imaging Protocols
Somatostatin analogues were stopped in patients receiving cold analog therapy before imaging: short-acting analogs for 3 days before scanning and long-acting analogs for 4-6 weeks. Fasting was not mandatory.
Each patient was administered the radiopharmaceutical of activity between 740 MBq and 925 MBq, which corresponded to 20 micrograms of Hynic TOC. The imaging was Repetition was prompted in case there were difficulties in the evaluation of the abdominal region, which usually resulted from the elimination of a part of the complex via the gastrointestinal (GI) tract. A whole-body scan and a single photon emission computed tomography (SPECT) acquisition in the region where the tumor was located (e.g., head, thorax, abdomen) was acquired. A dose of 370-550 MBq (10-15 mCi) of 99m Tc-Hynic TOC was injected IV. After a 60 to 90 minutes uptake period, patients underwent whole body scan followed by a regional SPECT/CT of the primary and metastatic sites. No contrast agent was used. The whole body images were acquired at a table speed of 8 centimeters per minute in a dual headed gamma camera (Siemens Symbia T equipped with an LEHR collimator, with energy peak of 140 Kev±15% window level).
In the SPECT/CT system, the CT acquisition was performed with a slice thickness of 4 mm and a pitch of 1 on a helical dual-slice CT unit. Images were acquired using a matrix of 512×512 pixels and a pixel size of 1 mm. Additional spot views were obtained when necessary. SPECT data were acquired using a matrix of 128×128 pixels and a slice thickness of 1.5 mm. CT-based attenuation correction of the emission images was used. SPECT images were reconstructed by iterative method ordered subset expectation maximization (2 iterations and 8 subsets).After completion of SPECT acquisition, the reconstructed attenuation corrected SPECT images, CT images, and fused images of matching pairs of SPECT and CT images were available for review in the axial, coronal, and sagital planes, as well as in maximum intensity projections and in the 3D cine mode.

Image Analysis
99m Tc-Hynic TOC planar and SPECT/CT studies were evaluated by two experienced nuclear medicine physicians in consensus. They were blinded to the findings of structural imaging. They evaluated the 99m Tc-Hynic TOC images both qualitatively and semi quantitatively. Any non physiologic focal area of increased 99m Tc-Hynic TOC uptake was sought. For 99m Tc-Hynic TOC, any non physiologic uptake that was greater than uptake in the surrounding area was interpreted as a positive finding for NET. Positive findings on 99m Tc-Hynic TOC were localized to anatomic images from the unenhanced CT study. The criteria for a correct detection of NET by 99m Tc-Hynic TOC are both positive 99m Tc-Hynic TOC uptakes and the correct anatomic localization of the tumor. The SPECT/CT findings were grouped as primary or metastatic disease. The maximum Tumor to background and tumor to normal liver ratios of primary lesions and metastatic lesions were calculated. For final analysis, the lesion with the highest pathologic tracer accumulation within each region in each patient was recorded.

Reference Standard
Histopathology results and the results of conventional imaging and follow-up imaging in combination with biochemical markers were used as the reference standard. Histopathologic confirmation was done for the primary site in most of the patients, which was not possible in all metastatic lesions because of technical or ethical reasons. Hence, few of the primary lesions and most of the metastatic lesions detected on 99m Tc-Hynic TOC were confirmed with conventional imaging and follow-up data, with ultrasound, or in the case of pancreatic lesions, with endoscopic ultrasound and biochemical markers. Conventional imaging modalities (contrast enhanced CT, MRI and ultrasound) reports were retrieved from the hospital database and reviewed for comparison.

Statistical Analysis
Continuous variables were expressed as medians and ranges. Categoric data were expressed as numbers and percentages. The sensitivity, specificity, accuracy, positive predictive value (PPV), and negative predictive value (NPV) of 99m Tc-Hynic TOC and conventional imaging modalities for detecting primary and metastatic lesions were calculated. The McNemar test was used to compare the diagnostic accuracy of 99m Tc-Hynic TOC with conventional imaging modalities. The Mann-Whitney test (two-tailed) was used to compare continuous variables. A P value of less than 0.05 was considered to be statistically significant. All the data analyses were performed using a statistical software package (SPSS, version 11.5, SPSS).

Patient Characteristics
A total of 22 patients with known gastroentero-pancreatic NET were included in the current study. Patient characteristics including age, sex, serum chromogranin a level, histology 34 Asia Oceania J Nucl Med Biol. 2014; 2(1):30-41.

Reference Standard
The reference standard for considering a lesion detected on 99m Tc-Hynic TOC planar or SPECT/ CT as either positive or negative for NET was based on a combination of the followings: histopathology results of the primary tumor in 16 patients (biopsy, n=10; fine-needle aspiration, n=6 patients), histopathology of metastatic lesions in 14 patients (biopsy, n=4 fine-needle aspiration, n=10 patients), follow-up 99m Tc-Hynic TOC planar or SPECT/ CT in 6 patients, correlation with conventional imaging (contrast enhanced CT or MRI) in 21 patients, biochemical marker in 19 patients, endoscopic ultrasound in 7 patients, and upper gastrointestinal endoscopy in 5 patients. Hence, in some patients, more than one method was used to confirm the diagnosis. Based on the reference standard, 16 patients had primary tumor and all 22 patients had metastases.

99m Tc-Hynic TOC planar or SPECT/ CT for Primary Tumor
99m Tc-Hynic TOC planar or SPECT/ CT detected primary tumor in 14 of 16 patients who had primary tumor according to the reference standard. A total of 15 primary tumors were localized in these 14 patients as 1 patient had 2 primary tumors ( Figure 1). The most common site of primary tumor was pancreas followed by duodenum (Table 2). In the remaining 2 patients, primary tumor was not localized by planar scintigraphy or SPECT/CT. The overall sensitivity, specificity, PPV, NPV, and accuracy of 99m Tc-Hynic TOC planar or SPECT/ CT for primary tumor are detailed in Table 3. 99m Tc-Hynic TOC planar or SPECT/ CT findings were true positive for primary tumor in 14 patients, It localized primary tumor in 8 patients with carcinoid, 4 patients with pancreatic NET, and 4 patients with NET not otherwise specified (NOS).   (Table 2). 99m Tc-Hynic TOC planar or SPECT/ CT findings were false negative for few of the liver metastases in 3 patient. The overall sensitivity, specificity, PPV, NPV, and accuracy of 99m Tc-Hynic TOC planar or SPECT/ CT for detecting metastases are detailed in Table 4. 99m Tc-Hynic TOC planar or SPECT/ CT was true-negative in 6 lesions and there was one false-positive lesion, when based on histopatholgy results or imaging follow up, where available.

Semi quantitative Analysis
Semi quantitative analysis (tumor to background and tumor to normal liver uptake ratios) of primary tumors and metastases were evaluated in all lesions. Among the primary tumors, histologic subtype did not influence the uptake of 99m Tc-Hynic TOC planar or SPECT/ CT. No significant difference was found in the uptake of carcinoid compared with pancreatic NET and NET NOS. Similarly, no significant difference was found between pancreatic NET and NET NOS.
However, the tumor to background and tumor to normal liver uptake   ratios of liver metastases was significantly higher than the uptake ratios of lymph node and bone metastases. No significant difference was found in uptake ratios between lymph node and bone metastases. Overall, no significant difference existed in uptake ratios of primary tumor and of metastases.

Conventional Imaging for Primary Tumor
Conventional imaging detected primary tumor in 7 of 16 patients who had primary tumor according to the reference standard. The overall sensitivity, specificity, PPV, NPV, and accuracy of conventional imaging for primary tumor are shown in Table 3. Conventional imaging findings were true positive for primary tumor in 7 patients, true-negative in 6.

Conventional Imaging for Metastases
Conventional imaging detected metastases in 18 of 22 patients who had one or more sites of metastasis according to the reference standard. A total of 34 lesions were noted in these 18 patients (Table 3). The most common site of metastases on conventional imaging was the liver (Figure 3), followed by the lymph nodes. The overall sensitivity, specificity, PPV, NPV, and accuracy of conventional imaging for detecting metastases are detailed in Table 4.

Comparison of 99m Tc-Hynic TOC planar or SPECT/ CT and Conventional Imaging for Primary Tumor
99m Tc-Hynic TOC planar or SPECT/ CT detected primary lesions in 14 patients compared with 7 patients on conventional imaging. In 2 patients, additional primary sites were detected with 99m Tc-Hynic TOC planar or SPECT/ CT. The total number of primary sites seen on 99m Tc-Hynic TOC planar or SPECT/ CT  30-41. 37 was 15, whereas 7 primary sites were seen by conventional imaging. 99m Tc-Hynic TOC planar or SPECT/ CT detected metastases in 22 patients compared with 18 patients on conventional imaging. A total of 56 metastatic regions were seen on 99m Tc-Hynic TOC planar or SPECT/ CT compared with 34 lesions on conventional imaging. In 8 patients, one or more additional metastatic sites were detected with 99m Tc-Hynic TOC planar or SPECT/ CT. On analysis, 99m Tc-Hynic TOC planar or SPECT/ CT was superior to conventional imaging for the detection of liver, lymph node and bone metastases.

Impact of 99m Tc-Hynic TOC planar or SPECT/ CT on Patient Management
Findings from this study led to a change in the management strategy in a number of patients. On the basis of the results, 6 patients (27.2%) underwent surgery for primary lesions that were not detected on other imaging modalities. In another 3 patients (13.6%), 99m Tc-Hynic TOC planar or SPECT/ CT helped in surgical planning by depicting additional surgically resectable sites. 9 patients (41%) were spared unnecessary surgery because evidence of the advanced stage of disease was seen. It changed the treatment regimen in 8 patients with liver metastases and ruled out liver metastases in one patient. In addition, the detection of the expression of somatostatin receptors in these patients led to the continuation of octreotide-based treatments. In 4 patients with progressive disease, imaging findings of strong receptor positivity led to peptide-based radionuclide therapy with 177 Lu DOTA-d-Phe(1)-Tyr(3)-Octreotate (TATE). Although continuation of treatment cannot be considered to be as management change, 99m Tc-Hynic TOC planar or SPECT/ CT definitely helped in supporting the treatment decisions in these patients (70%).

Discussion
In the past decade, SRS using 111 Inpentetreotide (OctreoScan) has played a central role in the functional assessment of NETs with a high degree of sensitivity and acceptable specificity for both primary as well as metastatic gastroenteropancreatic NETs. However, problems with SPECT emanate from the low resolution of the system that hampers imaging lesions that are small or have low receptor densities (35,36). More recently, the development of novel PET tracers ( 68 Ga-DOTA peptides) that bind specifically to somatostatin receptors expressed on the surface of NET cells allows the visualization of NET on 68 Ga-DOTApeptide PET/CT scans. Several different DOTA peptides (DOTA-d-Phe(1)-Tyr(3)-Octreotide [TOC], DOTA-NOC, and DOTA-TATE) have been used in this clinical setting for either NET diagnosis or peptide receptor radionuclide therapy. However the use of Gallium based somatostatin scintigraphy is restricted to centers with a PET-CT facility and is additionally expensive to procure the generator and post elution technology. Hence, the search for a suitable gamma camera based alternative is mandatory, to enable universal utilization of somatostatin scintigraphy for diagnosis and staging as well as a prelude to therapy.
Decristoforo et al preclinical studies (32)(33)(34) show that 99m Tc-Hynic TOC has important features in common with Octreoscan, (i.e., fast plasma clearance and, predominantly, urinary excretion). Moreover, the new tracer has advantages deriving from the optimal physical characteristics of being labeled with 99m Tc, improved scintigraphic image quality, availability and lower cost. In addition, as demonstrated by Maecke and Béhé (27) and Decristoforo (32), 99m Tc-Hynic TOC is characterized by a higher uptake in tumors than that of Octreoscan, especially when compared to the muscles and the heart.
Several studies in the past have established the efficacy of this tracer in NETs with varying results. In the current study, 99m Tc-Hynic TOC planar or SPECT/ CT showed a sensitivity of 87.5% and specificity of 85.7% for primary tumor.
Traditionally pancreatic NETs are usually well differentiated with a higher expression of somatostatin receptor subtype 2A (37,38). Most patients in the present study had well differentiated tumors with low Ki67 indices and differentiation grade 1-2, which might explain the high uptake even in metastatic lesions. The sensitivity and specificity of 99m Tc-Hynic TOC planar or SPECT/ CT for metastatic disease was 100% and 86%, respectively. This high sensitivity is consistent with high affinity somatostatin binding sites which have been found in vitro on most gastroenteropancreatic endocrine tumors (39,40). The majority of these tumors contain high numbers of receptors homogeneously distributed throughout the Asia Oceania J Nucl Med Biol. 2014; 2(1):30-41. tumor site. There was one false-positive study for primary tumor which was later confirmed to be physiologically high uptake in the uncinate process of the pancreas. Recent reviews routinely mention this finding of increased uptake in the head of pancreas as physiologic (41). 99m Tc-Hynic TOC planar or SPECT/ CT showed higher accuracy for both primary (87% vs 60%) and metastatic gastroenteropancreatic NETs (97% vs 75%) in comparison to conventional imaging modalities (P<0.0001). In seven patients, additional primary sites were detected with 99m Tc-Hynic TOC planar or SPECT/ CT. On lesion analysis, 99m Tc-Hynic TOC planar or SPECT/ CT was superior to conventional imaging for the detection of lymph node (P<0.0001) and bone (P=0.002) metastases ( Figure 4). However, no significant difference was found for liver metastases (P=1.000). In two patients with documented liver metastases 99m Tc-Hynic TOC planar or SPECT/ CT showed no uptake. This lack of uptake could be the result of poor differentiation of the lesions. Negative 99m Tc-Hynic TOC planar or SPECT/ CT findings are also crucial to select the appropriate therapy with combined chemotherapy using etoposide and cisplatin (42). In the current study, 99m Tc-Hynic TOC planar or SPECT/ CT had a significant impact on the management of patients with gastroenteropancreatic NETs. There was a substantial change in the management protocol for 6 patients (32%). 2 patients underwent surgery for primary lesions that were not detected on other conventional imaging modalities. One patient had confirmation of a primary tumor in the pancreas, which was suspected on conventional imaging. Other patients underwent resection of primary tumor based on 99m Tc-Hynic TOC imaging that was not detected on other modalities.
In 3 patients, 99m Tc-Hynic TOC planar or SPECT/ CT assisted in the evaluation of locoregional extension, which helped the surgeon to plan curative surgery. In 1 of these patients, additional primary foci were detected for surgical removal. In two patients, additional nodal disease was detected, which led to complete excision. 2 other patients were spared unnecessary surgery for the advanced stage of disease.
In one patient with a primary pancreatic gastrinoma, surgery was delayed because of 99m Tc-Hynic TOC upstaging with detection of liver metastases. Thus, there was an  30-41. 39 overall influence in almost half of the patients (42%) regarding management decisions (change in 32% and support in 10%). There have been reports of a kit formulation for the preparation of 99m Tc-Hynic TOC by Guggenberg et al (44). Though very simple to formulate, there were some limitations such as the lack of commercial kits in India, as well as a maximum of only two patient doses could be prepared using a single vial. The BARC kit is more versatile with capability of handling higher volumes of Technetium eluate, single step addition with no separate requirement for buffer solution, capability of handling up to 80 mCi (2,960 MBq) without compromising on radio chemical purity or image quality. The demonstration of quality of prepared product as well as high clinical performance in GPNET population will encourage 99m Tc-Hynic TOC application in neuro endocrine patients for staging and planning treatment. Especially in developing countries, where the patient load is high but centers with a PET CT facility or Germanium Gallium based imaging facilities are very few; this would be economically a much more viable alternative with equivalent diagnostic sensitivity and specificity. More investigations comparing the SPECT and PET radiopharmaceuticals are needed to further establish 99m Tc-Hynic TOC based imaging in the clinical algorithm.
A few limitations of the current study should be kept in mind. First, histopathologic confirmation of all lesions was not available. This was not technically or ethically feasible. Second, we could not compare the results with PET based somatostatin scintigraphy; which is currently considered the standard of care. Third, we did not attempt to reevaluate the conventional imaging modalities studies. Hence, we cannot comment on retrospective visibility of any lesion that was initially missed.

Conclusion
The newly developed lyophilized kits from BARC performed well in the clinical setting. 99m Tc-Hynic TOC planar or SPECT/ CT appears to be a highly sensitive and specific modality in the detection of gastroenteropancreatic NET. It is better than conventional imaging for this patient population and can have significant impact on patient management. The detection of a high degree of somatostatin receptor expression can be exploited to treat patients with cold octreotide therapy and peptide receptor radionuclide therapy, while a negative finding on 99m Tc-Hynic TOC planar or SPECT/ CT can guide the physician to choose an alternate form of treatment.